Canonical Allele Identifier: CA2612405473
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204388_9204398del , CM000673.2:g.9204388_9204398del GRCh38
NC_000011.9:g.9225935_9225945del , CM000673.1:g.9225935_9225945del GRCh37
NC_000011.8:g.9182511_9182521del NCBI36
NG_053019.1:g.65939_65949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.292-80_292-70del MANE Select ENSP00000328524.3:n.292-80_292-70del
ENST00000530780.2:c.*118-80_*118-70del ENSP00000433925.1:n.*118-80_*118-70del
ENST00000530867.2:n.81-80_81-70del
ENST00000532696.2:n.215-80_215-70del
ENST00000679446.1:n.213-80_213-70del
ENST00000679460.1:n.81-80_81-70del
ENST00000679568.1:c.292-80_292-70del ENSP00000505860.1:n.292-80_292-70del
ENST00000679745.1:n.81-80_81-70del
ENST00000679999.1:c.292-80_292-70del ENSP00000505198.1:n.292-80_292-70del
ENST00000680252.1:c.81-80_81-70del
ENST00000680294.1:c.292-80_292-70del ENSP00000506113.1:n.292-80_292-70del
ENST00000680470.1:c.292-80_292-70del ENSP00000505975.1:n.292-80_292-70del
ENST00000680554.1:c.4-80_4-70del ENSP00000505621.1:n.4-80_4-70del
ENST00000680576.1:n.81-80_81-70del
ENST00000680599.1:n.209-80_209-70del
ENST00000680742.1:c.292-80_292-70del ENSP00000505206.1:n.292-80_292-70del
ENST00000680885.1:n.213-80_213-70del
ENST00000681158.1:c.81-80_81-70del
ENST00000681173.1:n.81-80_81-70del
ENST00000681203.1:c.220-80_220-70del ENSP00000506456.1:n.220-80_220-70del
ENST00000681425.1:n.213-80_213-70del
ENST00000681915.1:n.81-80_81-70del
ENST00000328194.7:c.292-80_292-70del ENSP00000328524.3:n.292-80_292-70del
ENST00000526707.5:c.220-80_220-70del ENSP00000436780.1:n.220-80_220-70del
ENST00000530044.5:c.292-80_292-70del ENSP00000435866.1:n.292-80_292-70del
ENST00000530780.1:c.*118-80_*118-70del ENSP00000433925.1:n.*118-80_*118-70del
ENST00000532696.1:n.47-80_47-70del
NM_001243254.1:c.292-80_292-70del NP_001230183.1:n.292-80_292-70del
NM_015213.3:c.292-80_292-70del NP_056028.2:n.292-80_292-70del
XM_005252832.1:c.292-80_292-70del XP_005252889.1:n.292-80_292-70del
XM_011519952.1:c.292-80_292-70del XP_011518254.1:n.292-80_292-70del
XR_242782.2:n.557-80_557-70del
XR_930851.1:n.557-80_557-70del
XR_930852.1:n.557-80_557-70del
XR_930853.1:n.557-80_557-70del
NM_001348749.1:c.220-80_220-70del NP_001335678.1:n.220-80_220-70del
NM_001348750.1:c.4-80_4-70del NP_001335679.1:n.4-80_4-70del
NR_145966.2:n.549-80_549-70del
NM_015213.4:c.292-80_292-70del MANE Select NP_056028.2:n.292-80_292-70del
NM_001243254.2:c.292-80_292-70del NP_001230183.1:n.292-80_292-70del
NM_001348749.2:c.220-80_220-70del NP_001335678.1:n.220-80_220-70del
NM_001348750.2:c.4-80_4-70del NP_001335679.1:n.4-80_4-70del